Sideroblastic Anaemia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/BF00441138.pdf
Reference36 articles.
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2. Barosi G, Cazzola M, Morandi S, Stefanelli M, Perugini S (1978) Estimation of ferrokinetic parameters by a mathematical model in patients with Primary Acquired Sideroblastic Anaemia. Br J Haematol 39:409–423
3. Bottomley SS (1977) Porphyrin and iron metabolism in sideroblastic anemia. Semin Hematol 14:169–186
4. Buchanan GR, Bottomley SS, Niscke R (1980) Bone marrow delta aminolaevulinate synthase deficiency in a female with congenital sideroblastic Anaemia. Blood 55:109–116
5. Campbell BC, Meredith PA, Moore MR, Goldberg A (1978) Erythrocyte delta-aminolaevulinic acid dehydratase activity and changes in delta-aminolaevulinic acid concentrations in various forms of anaemia. Br J Haematol 40:397–400
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1. Arg452 substitution of the erythroid-specific 5-aminolaevulinate synthase, a hot spot mutation in X-linked sideroblastic anaemia, does not itself affect enzyme activity;European Journal of Haematology;2006-01
2. Pyridoxine responsive sideroblastic anemia in a boy with mitral valve prolapse;Korean Journal of Pediatrics;2006
3. Hypoplastic anemia;Neonatal Hematology;2005-08-18
4. Pyridoxine-refractory congenital sideroblastic anaemia with evidence for autosomal inheritance: exclusion of linkage to ALAS2 at Xp11.21 by polymorphism analysis.;Journal of Medical Genetics;1994-03-01
5. Does Rapidly Progressive Iron Overload in a Young Girl with Sideroblastic Anemia Also Signify the Presence of Hereditary Hemochromatosis?;Pediatric Hematology and Oncology;1994-01
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